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      • Spring, Texas
      • Temp to Perm
      • $17.00 - $18.00 per hour
      • 6:00 AM - 3:00 PM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to ensure purity of research and GMP materials.Responsibilities:*Maintain, clean, and sterilize manufacturing equipment.*Maintain highest standard of clean room environment in order to ensure purity of lab work.*Perform preventative maintenance.*Document activities for GMP materials.*Manage supplies inventory.Working hours: 6:00 AM - 3:00 PMSkills:*Organization*Attention to detail*DocumentationEducation:High SchoolExperience:0-1 yearsQualifications:*High school diploma or general education degree (GED); or one to three months related experience and/or training*Experience working in a GMP facility or pharmaceutical environment is preferred www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to ensure purity of research and GMP materials.Responsibilities:*Maintain, clean, and sterilize manufacturing equipment.*Maintain highest standard of clean room environment in order to ensure purity of lab work.*Perform preventative maintenance.*Document activities for GMP materials.*Manage supplies inventory.Working hours: 6:00 AM - 3:00 PMSkills:*Organization*Attention to detail*DocumentationEducation:High SchoolExperience:0-1 yearsQualifications:*High school diploma or general education degree (GED); or one to three months related experience and/or training*Experience working in a GMP facility or pharmaceutical environment is preferred www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • Spring, Texas
      • Temp to Perm
      • $20.00 - $23.00 per hour
      • 8:00 AM - 5:00 PM
      The primary purpose of the Production Planner is to coordinate production for multiple planned projects and products. The Production Planner will be responsible for planning and prioritization of applicable operations and meeting deadlines.Responsibilities:* Coordinate workflows* Ensure production performance and monitor production performance in a timely manner. * Determine production materials needed.* Approve manufacturing orders.* Utilize ERP software to set up items and Bill of Material.* Problem resolution and determination of priorities. *Communicate support functions. * Ensure proper inventory levels. * Document status and performance reports. * Author SOPs and compose reports.* Inventory counts.Working hours: 8:00 AM - 5:00 PMSkills:* Microsoft Suites* Professional verbal and writing skills.* Understanding of Manufacturing processes and time management. * Supply chain experience with ERP software.* Experience with Oracle, NetSuite preferred.Education:High SchoolExperience:1-4 yearsQualifications:* GMP experience.* High School Diploma or GED* 3 - 5 years Production Planning or Pharmaceuticals Manufacturing environment experience. www.spherion.comSpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      The primary purpose of the Production Planner is to coordinate production for multiple planned projects and products. The Production Planner will be responsible for planning and prioritization of applicable operations and meeting deadlines.Responsibilities:* Coordinate workflows* Ensure production performance and monitor production performance in a timely manner. * Determine production materials needed.* Approve manufacturing orders.* Utilize ERP software to set up items and Bill of Material.* Problem resolution and determination of priorities. *Communicate support functions. * Ensure proper inventory levels. * Document status and performance reports. * Author SOPs and compose reports.* Inventory counts.Working hours: 8:00 AM - 5:00 PMSkills:* Microsoft Suites* Professional verbal and writing skills.* Understanding of Manufacturing processes and time management. * Supply chain experience with ERP software.* Experience with Oracle, NetSuite preferred.Education:High SchoolExperience:1-4 yearsQualifications:* GMP experience.* High School Diploma or GED* 3 - 5 years Production Planning or Pharmaceuticals Manufacturing environment experience. www.spherion.comSpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • Spring, Texas
      • Temp to Perm
      • $18.00 - $20.00 per hour
      • 8:00 AM - 5:00 PM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. Responsible for the maintenance, cleaning, and sterilization of equipment, supplies, and production areas.Responsibilities:* Wash glassware, plastic supplies, and other supporting equipment in a washer or by hand,as needed.* Sterilize materials to support PD/HD manufacture, testing and research.* Weekly and daily cleaning and disinfection of the PD production areas,including documentation of cleaning performed.* Restock main supplies in Production Areas*Perform basic in-process yield analysis of PD and MFG samples, including Miniprep andGel ElectrophoresisWorking hours: 8:00 AM - 5:00 PMSkills:*Lab maintenance and care*Clean room experienceEducation:High SchoolExperience:0-1 yearsQualifications:*1-3 Months related experience or training*Life Sciences background preferred. www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. Responsible for the maintenance, cleaning, and sterilization of equipment, supplies, and production areas.Responsibilities:* Wash glassware, plastic supplies, and other supporting equipment in a washer or by hand,as needed.* Sterilize materials to support PD/HD manufacture, testing and research.* Weekly and daily cleaning and disinfection of the PD production areas,including documentation of cleaning performed.* Restock main supplies in Production Areas*Perform basic in-process yield analysis of PD and MFG samples, including Miniprep andGel ElectrophoresisWorking hours: 8:00 AM - 5:00 PMSkills:*Lab maintenance and care*Clean room experienceEducation:High SchoolExperience:0-1 yearsQualifications:*1-3 Months related experience or training*Life Sciences background preferred. www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • Spring, Texas
      • Temp to Perm
      • $19.00 - $20.00 per hour
      • 8:00 AM - 5:00 AM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to ensure compliance with regulatory requirements and internal policies in the manufacturing department.Responsibilities:*Review all batch documentation.*Review production records. *Endorse documentation in compliance with regulations and company QC guidelines.*Assist in reviewing and writing SOPs for manufacturing.* Write and review protocols for development, Installation Qualification and Operational Qualification.*Write and review protocol validations.*Assist in routine company audits.*Review deviations and investigations.*Write and review protocols for development reports.* Ensure compliance with GMPs SOPs.Working hours: 8:00 AM - 5:00 AMSkills:*Excellent written and oral communication skills.*Meticulous organizational skills.*Meticulous documentation and record review practices.*Technical writing experience.Education:BachelorsExperience:1-4 yearsQualifications:*Associate's degree and/or one to three years of relevant experience.*Must have previous technical writing experience in a lab setting. *Experience working in a GMP facility or pharmaceutical environment.*Biology or related life sciences as related to manufacture of plasmid DNA. www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to ensure compliance with regulatory requirements and internal policies in the manufacturing department.Responsibilities:*Review all batch documentation.*Review production records. *Endorse documentation in compliance with regulations and company QC guidelines.*Assist in reviewing and writing SOPs for manufacturing.* Write and review protocols for development, Installation Qualification and Operational Qualification.*Write and review protocol validations.*Assist in routine company audits.*Review deviations and investigations.*Write and review protocols for development reports.* Ensure compliance with GMPs SOPs.Working hours: 8:00 AM - 5:00 AMSkills:*Excellent written and oral communication skills.*Meticulous organizational skills.*Meticulous documentation and record review practices.*Technical writing experience.Education:BachelorsExperience:1-4 yearsQualifications:*Associate's degree and/or one to three years of relevant experience.*Must have previous technical writing experience in a lab setting. *Experience working in a GMP facility or pharmaceutical environment.*Biology or related life sciences as related to manufacture of plasmid DNA. www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • Spring, Texas
      • Temp to Perm
      • $25.00 - $29.00 per hour
      • 6:00 AM - 3:00 PM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to supervise department personnel and manufacture plasmid DNA in accordance with cGMP guidelines.Responsibilities:*Oversee employees.*Ensure highest quality team work completed during manufacture of plasmid DNA.*Assist in scaling-up processes.*Manufacture plasmid DNA.*Cell banking and fermentation following SOPs and cGMP guidelines.* Purification processes following SOPs and cGMP guidelines.* Ensure team is working in accordance with cGMP guidelines.* Prepare solutions to be used in the manufacturing process.*Implement validation protocols.*Write SOPs.*Lab equipment maintenance.Working hours: 6:00 AM - 3:00 PMSkills:*Established expertise in biological science or related life sciences. *Possess leadership skills and the ability to lead a team in a laboratory setting.*Excellent written and oral communication skills.*Ability to work in a clean room environment for extended periods of time.*Ability to wear and work in PPE.Education:AssociateExperience:1-4 yearsQualifications:* Bachelors or Associates degree in a life science related field with 3 or more years of cGMP manufacturing experience* Plasmid purification experience* Knowledge of microbiological techniques www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to supervise department personnel and manufacture plasmid DNA in accordance with cGMP guidelines.Responsibilities:*Oversee employees.*Ensure highest quality team work completed during manufacture of plasmid DNA.*Assist in scaling-up processes.*Manufacture plasmid DNA.*Cell banking and fermentation following SOPs and cGMP guidelines.* Purification processes following SOPs and cGMP guidelines.* Ensure team is working in accordance with cGMP guidelines.* Prepare solutions to be used in the manufacturing process.*Implement validation protocols.*Write SOPs.*Lab equipment maintenance.Working hours: 6:00 AM - 3:00 PMSkills:*Established expertise in biological science or related life sciences. *Possess leadership skills and the ability to lead a team in a laboratory setting.*Excellent written and oral communication skills.*Ability to work in a clean room environment for extended periods of time.*Ability to wear and work in PPE.Education:AssociateExperience:1-4 yearsQualifications:* Bachelors or Associates degree in a life science related field with 3 or more years of cGMP manufacturing experience* Plasmid purification experience* Knowledge of microbiological techniques www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • Spring, Texas
      • Temp to Perm
      • $20.00 - $23.00 per hour
      • 8:00 AM - 5:00 PM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to review documentation of the Process Development team to ensure compliance with regulatory requirements.Responsibilities:* Review for compliance and approve all documentation for Research Grade and Highly Documented products.* Write up deviations and investigations.* Write and review all SOPs for Process Development team.* Review records related to production and process development. * Follow GMPs and SOPs to ensure company compliance. * Maintain applicable product inventories.* Summarize data.* Write Plasmid DNA evaluation summaries.Working hours: 8:00 AM - 5:00 PMSkills:* Must have previous technical writing experience in a lab setting.* Experience working in a GMP facility or pharmaceutical environment.* Experience with GMPs and SOPs as applicable to manufacture of Plasmid DNA* Technical writing and reviewing abilities. * Attention to detail and commitment to compliance.* Ability to identify and document scientific deviations.* Inventory maintenance.Education:AssociateExperience:1-4 yearsQualifications:* Associates degree.* Between 1 - 3 years experience in related role. www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to review documentation of the Process Development team to ensure compliance with regulatory requirements.Responsibilities:* Review for compliance and approve all documentation for Research Grade and Highly Documented products.* Write up deviations and investigations.* Write and review all SOPs for Process Development team.* Review records related to production and process development. * Follow GMPs and SOPs to ensure company compliance. * Maintain applicable product inventories.* Summarize data.* Write Plasmid DNA evaluation summaries.Working hours: 8:00 AM - 5:00 PMSkills:* Must have previous technical writing experience in a lab setting.* Experience working in a GMP facility or pharmaceutical environment.* Experience with GMPs and SOPs as applicable to manufacture of Plasmid DNA* Technical writing and reviewing abilities. * Attention to detail and commitment to compliance.* Ability to identify and document scientific deviations.* Inventory maintenance.Education:AssociateExperience:1-4 yearsQualifications:* Associates degree.* Between 1 - 3 years experience in related role. www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • Spring, Texas
      • Temp to Perm
      • $30.00 - $32.00 per hour
      • 8:00 AM - 5:00 PM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to work as liaison between clients and applicable company departments in order to ensure project success. The Client Project Manager is expected to monitor all projects and maintain they fall within applicable budget and time constraints.Responsibilities:* Work with clients as a direct contact representing company departments and interests as pertains to company projects. * Assist in project development and objectives while maintaining correspondence with all applicable points of contact involved in the project.* Develop mappable project plans in order to share with clients and staff. * Track the progression of projects and monitor project success and completion of predetermined goals.* Use company tools and systems in order to accurately assess client and customer feedback.* Develop and maintain accurate documentation of project processes and statuses.* Make changes to project constraints with the intention of meeting budget objectives after financial analysis has been conducted. * Maintain recurring and ongoing communication with all relevant personnel and clients and provide updates on all aspects of the project.Working hours: 8:00 AM - 5:00 PMSkills:* Microsoft Office; Word, PowerPoint, and Excel* Project Development and Management* Professional written and verbal communication skills. * Advanced Client and Vendor RelationsEducation:BachelorsExperience:1-4 yearsQualifications:* Bachelor's degree in applicable life sciences. * 2 - 4 years experience in project/account management. * Experience in pharmaceutical industry is preferred. www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to work as liaison between clients and applicable company departments in order to ensure project success. The Client Project Manager is expected to monitor all projects and maintain they fall within applicable budget and time constraints.Responsibilities:* Work with clients as a direct contact representing company departments and interests as pertains to company projects. * Assist in project development and objectives while maintaining correspondence with all applicable points of contact involved in the project.* Develop mappable project plans in order to share with clients and staff. * Track the progression of projects and monitor project success and completion of predetermined goals.* Use company tools and systems in order to accurately assess client and customer feedback.* Develop and maintain accurate documentation of project processes and statuses.* Make changes to project constraints with the intention of meeting budget objectives after financial analysis has been conducted. * Maintain recurring and ongoing communication with all relevant personnel and clients and provide updates on all aspects of the project.Working hours: 8:00 AM - 5:00 PMSkills:* Microsoft Office; Word, PowerPoint, and Excel* Project Development and Management* Professional written and verbal communication skills. * Advanced Client and Vendor RelationsEducation:BachelorsExperience:1-4 yearsQualifications:* Bachelor's degree in applicable life sciences. * 2 - 4 years experience in project/account management. * Experience in pharmaceutical industry is preferred. www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • Spring, Texas
      • Temp to Perm
      • $23.00 - $25.00 per hour
      • 8:00 AM - 5:00 PM
      The primary purpose of this position is to ensure quality assurance and compliance activities. This person will be responsible for production, testing, and associated documentation is within industry guidelines.Responsibilities:*Assemble applicable documentation *Process CAPAs and perform routine internal audits and maintain quality control.*Maintaining supplier files and audits*Proper documentation of equipment *Training new employees*Develop quality system SOPs*Inventory Products *Follow (GMPs) and (SOPs)*Review and approve Analysis Certificates*Print and approve product labelsWorking hours: 8:00 AM - 5:00 PMSkills:*Plasmid purification and microbiology techniques *Quality Assurance documentationEducation:BachelorsExperience:4-7 yearsQualifications:*GMP experience*Bachelors degree in applicable life science field www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      The primary purpose of this position is to ensure quality assurance and compliance activities. This person will be responsible for production, testing, and associated documentation is within industry guidelines.Responsibilities:*Assemble applicable documentation *Process CAPAs and perform routine internal audits and maintain quality control.*Maintaining supplier files and audits*Proper documentation of equipment *Training new employees*Develop quality system SOPs*Inventory Products *Follow (GMPs) and (SOPs)*Review and approve Analysis Certificates*Print and approve product labelsWorking hours: 8:00 AM - 5:00 PMSkills:*Plasmid purification and microbiology techniques *Quality Assurance documentationEducation:BachelorsExperience:4-7 yearsQualifications:*GMP experience*Bachelors degree in applicable life science field www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • Spring, Texas
      • Temp to Perm
      • $20.00 - $24.00 per hour
      • 8:00 AM - 5:00 PM
      This primary purpose of the Validation Specialist will be to support production and product quality. Verification and validation of equipment and documentation and products to ensure products are in accordance with company requirements.Responsibilities:* Support validation by developing validation documentation protocols and executing them.* Compiling data and authoring reports*Support new products, optimize processes, and technology transfers.*Support Quality Control and validate assays.*Support Quality Control instrumentation.* Participate in team projects in order to implement product development. * Maintain process and validation schedules and filing to company standards.* Training of staff and team growth support. * Stay current of all process technology and recommend improvements as needed. * Report to Quality Assurance manager status of Operations.Working hours: 8:00 AM - 5:00 PMSkills:* Validation and re-Validation of Quality Control assays preferred. * Qualification and re-Qualification of Quality Control testing and instrumentation preferred. * GMP experience. * Experience in Pharmaceutical and Biologics preferred.Education:BachelorsExperience:1-4 yearsQualifications:* 1 - 3 years applicable experience.* Bachelor's degree in Life Sciences field, or experience or training in a Pharmaceutical or Biologics environment. www.spherion.comSpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      This primary purpose of the Validation Specialist will be to support production and product quality. Verification and validation of equipment and documentation and products to ensure products are in accordance with company requirements.Responsibilities:* Support validation by developing validation documentation protocols and executing them.* Compiling data and authoring reports*Support new products, optimize processes, and technology transfers.*Support Quality Control and validate assays.*Support Quality Control instrumentation.* Participate in team projects in order to implement product development. * Maintain process and validation schedules and filing to company standards.* Training of staff and team growth support. * Stay current of all process technology and recommend improvements as needed. * Report to Quality Assurance manager status of Operations.Working hours: 8:00 AM - 5:00 PMSkills:* Validation and re-Validation of Quality Control assays preferred. * Qualification and re-Qualification of Quality Control testing and instrumentation preferred. * GMP experience. * Experience in Pharmaceutical and Biologics preferred.Education:BachelorsExperience:1-4 yearsQualifications:* 1 - 3 years applicable experience.* Bachelor's degree in Life Sciences field, or experience or training in a Pharmaceutical or Biologics environment. www.spherion.comSpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.

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